Ale intervertebral fusion device system - Taiwan Registration 5bc96fbdd9efd89bc5a0727cb234b260
Access comprehensive regulatory information for Ale intervertebral fusion device system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bc96fbdd9efd89bc5a0727cb234b260 and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone Biotechnology Co.,Ltd..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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5bc96fbdd9efd89bc5a0727cb234b260
Registration Details
Taiwan FDA Registration: 5bc96fbdd9efd89bc5a0727cb234b260
Device Details
Ale intervertebral fusion device system
TW: ไบๆจๆค้่ๅๅจ็ณป็ตฑ
Risk Class 2

